Canonical Allele Identifier: CA2184071747
Gene: MAP2K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66435118_66435121delinsCAGA , CM000677.2:g.66435118_66435121delinsCAGA GRCh38
NC_000015.9:g.66727456_66727459delinsCAGA , CM000677.1:g.66727456_66727459delinsCAGA GRCh37
NC_000015.8:g.64514510_64514513delinsCAGA NCBI36
NG_008305.1:g.53246_53249delinsCAGA , LRG_725:g.53246_53249delinsCAGA

Transcript Alleles

HGVS Amino-acid change
ENST00000684779.1:c.106_109delinsCAGA ENSP00000508681.1:p.Gln36=
ENST00000685172.1:c.172_175delinsCAGA ENSP00000509604.1:p.Gln58=
ENST00000685763.1:c.172_175delinsCAGA ENSP00000509016.1:p.Gln58=
ENST00000686347.1:c.172_175delinsCAGA ENSP00000509027.1:p.Gln58=
ENST00000687191.1:n.608_611delinsCAGA
ENST00000689951.1:c.172_175delinsCAGA ENSP00000509308.1:p.Gln58=
ENST00000691077.1:c.172_175delinsCAGA ENSP00000509843.1:p.Gln58=
ENST00000691576.1:c.172_175delinsCAGA ENSP00000510066.1:p.Gln58=
ENST00000691937.1:c.172_175delinsCAGA ENSP00000508768.1:p.Gln58=
ENST00000692487.1:c.172_175delinsCAGA ENSP00000509534.1:p.Gln58=
ENST00000692683.1:c.106_109delinsCAGA ENSP00000508437.1:p.Gln36=
ENST00000693150.1:c.106_109delinsCAGA ENSP00000510309.1:p.Gln36=
ENST00000307102.10:c.172_175delinsCAGA MANE Select ENSP00000302486.5:p.Gln58=
ENST00000307102.9:c.172_175delinsCAGA ENSP00000302486.4:p.Gln58=
ENST00000425818.2:n.683_686delinsCAGA
NM_002755.3:c.172_175delinsCAGA , LRG_725t1:c.172_175delinsCAGA NP_002746.1:p.Gln58=
XM_011521783.1:c.106_109delinsCAGA XP_011520085.1:p.Gln36=
XM_011521783.3:c.106_109delinsCAGA XP_011520085.1:p.Gln36=
XM_017022411.2:c.172_175delinsCAGA XP_016877900.1:p.Gln58=
XM_017022412.1:c.106_109delinsCAGA XP_016877901.1:p.Gln36=
NM_002755.4:c.172_175delinsCAGA MANE Select NP_002746.1:p.Gln58=